# K113303: Osleobridge Idsf Spacer Conector

- Pathway: 510(k) (Special)
- Applicant: Merete Medical GmbH
- Decided: Dec 9, 2011 after 30 days
- Product code: HSB (Rod, Fixation, Intramedullary And Accessories)
- Device class: 2
- Regulation: 21 CFR 888.3020
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K142451: OsteoBridge IDSF - Intramedullary Diaphyseal Segmental Defect Fixation Rod System (2015), 1 descendant of its own
- K181026: OsteoBridge™ IDSF System (2018), 0 descendants of its own

## Indications for use
The device is intended to be used in the management of segmental diaphyseal bone loss of either humerus or tibia or femur in oncology patients secondary to radical bone loss and/or resection due to tumors. The intramedullary rods can be fixed with interlocking screws without or with bone cement.

Source page: https://510kreport.com/device/K113303
Methodology: https://510kreport.com/methodology